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250937

Sigma-Aldrich

1,6-Dimethylnaphthalene

99%

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About This Item

Linear Formula:
C10H6(CH3)2
CAS Number:
575-43-9
Molecular Weight:
156.22
Beilstein:
1854429
EC Number:
209-385-1
MDL number:
MFCD00004039
UNSPSC Code:
12352100
PubChem Substance ID:
24855083
NACRES:
NA.22

Quality Level

100

Assay

99%

refractive index

n20/D 1.606 (lit.)

bp

265-266 °C (lit.)

mp

−17-−16 °C (lit.)

density

1.002 g/mL at 25 °C (lit.)

SMILES string

Cc1ccc2c(C)cccc2c1

InChI

1S/C12H12/c1-9-6-7-12-10(2)4-3-5-11(12)8-9/h3-8H,1-2H3

InChI key

CBMXCNPQDUJNHT-UHFFFAOYSA-N

Gene Information

human ... CYP1A2(1544)

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Storage Class Code

10 - Combustible liquids

WGK

WGK 3

Flash Point(F)

233.6 °F - closed cup

Flash Point(C)

112 °C - closed cup

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

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Loaded liquid scintillators based on 1, 6-dimethylnaphthalene and 1-methylnaphthalene.
Koike Y and Yamamoto K.
Nuclear Instruments and Methods in Physics Research, 84(1), 24-28 (1970)
The assessment of some volatile organic compounds as sprout suppressants for ware and seed potatoes.
Beveridge JL, et al.
Potato Research, 24(1), 61-76 (1981)
Nien-Hsin Kao et al.
Marine pollution bulletin, 97(1-2), 319-332 (2015-06-08)
Three fishing harbors were investigated to study the polycyclic aromatic hydrocarbons in the sediments and trace possible anthropogenic sources by identification of cyclic terpenoid biomarkers. Seventeen terpanes, 10 steranes and 10 bicyclic sesquiterpanes in the marine diesel and the three
Kunal Roy et al.
European journal of medicinal chemistry, 44(5), 1941-1951 (2008-12-27)
A series of naphthalene and non-naphthalene derivatives (n=42) having cytochrome P450 2A6 and 2A5 inhibitory activities, reported by Rahnasto et al., were subjected to QSAR and QAAR studies. The analyses were performed using electronic, spatial, shape and thermodynamic descriptors to
Laura E Korhonen et al.
Journal of medicinal chemistry, 48(11), 3808-3815 (2005-05-27)
The purpose of this study was to determine the cytochrome P450 1A2 (CYP1A2) inhibition potencies of structurally diverse compounds to create a comprehensive three-dimensional quantitative structure-activity relationship (3D-QSAR) model of CYP1A2 inhibitors and to use this model to predict the
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